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Effects of Inspiratory Muscle Training on Postural Stability, Balance, Pulmonary Function and Functional Capacity in Children With Cystic Fibrosis

Effects of Inspiratory Muscle Training on Postural Stability, Balance, Pulmonary Function and Functional Capacity in Children With Cystic Fibrosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03375684
Enrollment
32
Registered
2017-12-18
Start date
2018-01-02
Completion date
2018-05-21
Last updated
2018-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

Cystic Fibrosis, Inspiratory Muscle Training, Chest Physiotherapy, Balance, Postural Stability, Pulmonary Function Test, 6-Minute Walk Test

Brief summary

It is extensively reported in the literature that patients with chronic obstructive lung disease may have impairments in balance and postural control which further increase the disease burden. Mechanisms related to these impairments include, but are not limited to increased work of breathing, diaphragm weakness, peripheral muscle weakness and systemic inflammation. Since the similar symptoms are reported for the children with cystic fibrosis, it is hypothesized that balance and postural control may also be compromised in these patients. Inspiratory muscle training (IMT) is shown to improve diaphragm strength and pulmonary function. Considering the relation between diaphragm which is one of the core muscles, and balance, IMT may also have an impact on postural control and balance alongside the standard clinical parameters such as respiratory muscle strength, pulmonary function and functional capacity in these patients. Thus, the aim of this study was to investigate the effects of inspiratory muscle training and conventional chest physiotherapy on postural stability, balance, pulmonary function and functional capacity in children with cystic fibrosis.

Interventions

Programme will include diaphragmatic breathing exercise, thoracic expansion exercises, incentive spirometer exercise (Triflo), oscillatory PEP (Flutter), postural drainage and coughing tecniques.

OTHERInspiratory muscle training

Threshold IMT device will be used for the training. Training intensity will set at 30% of the maximum inspiratory pressure.

Sponsors

Bezmialem Vakif University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
8 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Cystic fibrosis diagnosis * Stable clinical condition (no exacerbation in last 4 weeks)

Exclusion criteria

* Documented diagnosis of vestibular, neurological or orthopedic disorders which may affect balance and mobility * Subjects previously involved in exercise training or physiotherapy programs

Design outcomes

Primary

MeasureTime frame
Change from baseline distance covered in six-minute walk test at 8 weeksEight weeks
Change from baseline postural stability test score in Biodex Balance System SD at 8 weeksEight weeks
Change from baseline limits of stability test score in Biodex Balance System SD at 8 weeksEight weeks
Change from baseline sensory integriation and balance test score in Biodex Balance System SD at 8 weeksEight weeks
Change from baseline Forced Vital Capacity (FVC) at 8 weeksEight weeks
Change from baseline Forced Expiratory Volume in 1 second (FEV1) at 8 weeksEight weeks
Change from baseline Peak Expiratory Flow (PEF) at 8 weeksEight weeks
Change from baseline maximum inspiratory pressure at 8 weeksEight weeks
Change from baseline maximum expiratory pressure at 8 weeksEight weeks

Secondary

MeasureTime frame
Change from baseline m. quadriceps strength at 8 weeksEight weeks

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026